Head of Medical Device Lab – Senior Manager, GMP Testing

Novartis

Schweiz

Hybrid

EUR 66.000 - 118.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden
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Benefits dieser Stelle

Hybrid work model
World-wide career possibilities within
Company pension scheme
Learning and development opportunities

Zusammenfassung

Novartis seeks a Senior Manager - Head of Medical Device Laboratory in Schaftenau, Austria, to lead the Analytical Innovation & Testing team. You will drive method development, validation and transfer for functional tests of combination products, ensuring GMP-compliant documentation and strong project delivery.

The role requires a Master’s/PhD in a relevant field, proven leadership, and experience with regulatory guidelines for drug-device products.

Qualifikationen

  • Master's or PhD in natural science, engineering or pharmaceutical field or equivalent.
  • Strong leadership and people-management abilities.
  • Experience with regulatory guidelines for drug-device products (ISO, cGMP).
  • Excellent organizational and communication skills, self-motivated and collaborative.

Aufgaben

  • Lead the Analytical Innovation & Testing team in Schaftenau.
  • Plan, manage, and control project resources, schedules, and budgets.
  • Oversee method development for functional tests for combination products per ISO and pharmacopeia requirements.
  • Ensure GMP-compliant documentation and Design Control alignment.
  • Act as Head of Quality Control under AMBO §9 and support inspections.

Kenntnisse

People leadership
Project planning
Communication skills
Regulatory awareness
English fluency

Ausbildung

Master's or PhD in natural science or engineering

Jobbeschreibung

Novartis seeks a Senior Manager - Head of Medical Device Laboratory in Schaftenau, Austria, to lead the Analytical Innovation & Testing team. You will drive method development, validation and transfer for functional tests of combination products, ensuring GMP-compliant documentation and strong project delivery.

The role requires a Master’s/PhD in a relevant field, proven leadership, and experience with regulatory guidelines for drug-device products.

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